Stargardt disease
Stargardt disease
Definition
Stargardt disease, also known as Stargardt 1 (STGD1), is an autosomal recessive form of retinal dystrophy that is usually characterized by a progressive loss of central vision associated with irregular macular and perimacular yellow-white fundus flecks, and a so-called ''beaten bronze'' atrophic central macular lesion.
Also known as fundus flavimaculatus, Stargardt 1 — per MONDO
Also identified as
- DOID 0050817 per MONDO
- MESH D000080362 per MONDO
- NCIT C85078 per MONDO
- Orphanet 827 per MONDO
- SCTID 47673003 per MONDO
- UMLS C0271093 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Camera-type eye | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Camera-type eye | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Retina | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Retina | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |